P184
P40
Initial sequencing and analysis of the human genomeUsing GeneWise in the Drosophila annotation experimentGeneWise and GenomewiseThe genome sequence of Caenorhabditis briggsae: a platform for comparative genomicsThe Sequence Ontology: a tool for the unification of genome annotationsTrait variation in yeast is defined by population historyHigh levels of RNA-editing site conservation amongst 15 laboratory mouse strainsA genome-wide survey of genetic variation in gorillas using reduced representation sequencingQuantitative genetics of CTCF binding reveal local sequence effects and different modes of X-chromosome associationThe DNA sequence and biological annotation of human chromosome 1The DNA sequence and comparative analysis of human chromosome 10The DNA sequence and analysis of human chromosome 6The DNA sequence and comparative analysis of human chromosome 20The DNA sequence of the human X chromosomeDNA sequence and analysis of human chromosome 9The diploid genome sequence of an Asian individualA systematic comparative and structural analysis of protein phosphorylation sites based on the mtcPTM databaseEnsembl 2008An integrated map of genetic variation from 1,092 human genomesInsights into hominid evolution from the gorilla genome sequencePopulation genomics of domestic and wild yeastsGenome sequence of the Brown Norway rat yields insights into mammalian evolutionSystematic analysis of human protein complexes identifies chromosome segregation proteinsThe Ensembl genome database projectThe Pfam protein families databaseWormBase: network access to the genome and biology of Caenorhabditis elegansRNA sequence analysis using covariance modelsEnsembl 2011A map of human genome variation from population-scale sequencingEfficient de novo assembly of large genomes using compressed data structuresAccurate whole human genome sequencing using reversible terminator chemistryWormBase: a comprehensive resource for nematode researchEnsembl's 10th yearEnsemblCompara GeneTrees: Complete, duplication-aware phylogenetic trees in vertebratesMapping short DNA sequencing reads and calling variants using mapping quality scoresThe DNA sequence and analysis of human chromosome 13TreeFam: 2008 UpdateA Bayesian deconvolution strategy for immunoprecipitation-based DNA methylome analysisIdentification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencingFast and accurate short read alignment with Burrows-Wheeler transform
P50
description
British computational biologist
@en
name
Richard M. Durbin
@ast
Richard M. Durbin
@ca
Richard M. Durbin
@da
Richard M. Durbin
@de
Richard M. Durbin
@en
Richard M. Durbin
@es
Richard M. Durbin
@fo
Richard M. Durbin
@fr
Richard M. Durbin
@hu
Richard M. Durbin
@is
type
label
Richard M. Durbin
@ast
Richard M. Durbin
@ca
Richard M. Durbin
@da
Richard M. Durbin
@de
Richard M. Durbin
@en
Richard M. Durbin
@es
Richard M. Durbin
@fo
Richard M. Durbin
@fr
Richard M. Durbin
@hu
Richard M. Durbin
@is
altLabel
Richard Durbin
@de
Richard Durbin
@en
Richard Michael Durbin
@en
prefLabel
Richard M. Durbin
@ast
Richard M. Durbin
@ca
Richard M. Durbin
@da
Richard M. Durbin
@de
Richard M. Durbin
@en
Richard M. Durbin
@es
Richard M. Durbin
@fo
Richard M. Durbin
@fr
Richard M. Durbin
@hu
Richard M. Durbin
@is